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4-Bromo-7-methyl-1H-indole is a chemical compound with the molecular formula C9H8BrN, belonging to the indole family of heterocyclic aromatic compounds. It is a derivative of indole, which is commonly found in natural products such as tryptophan and serotonin. This versatile chemical is characterized by the presence of a bromine atom at the 4-position and a methyl group at the 7-position, which contribute to its unique properties and applications.

936092-87-4

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936092-87-4 Usage

Uses

Used in Pharmaceutical Synthesis:
4-Bromo-7-methyl-1H-indole is used as a building block in the synthesis of pharmaceuticals, particularly for the development of new drug candidates. Its unique structure allows for the formation of carbon-carbon bonds and other chemical reactions, facilitating the creation of diverse and effective pharmaceutical compounds.
Used in Agrochemical Synthesis:
In addition to its applications in pharmaceuticals, 4-Bromo-7-methyl-1H-indole is also utilized as a building block in the synthesis of agrochemicals. Its chemical properties make it suitable for the development of new agrochemicals with improved efficacy and selectivity.
Used in Organic Chemistry Reactions:
4-Bromo-7-methyl-1H-indole serves as a valuable reagent in various organic chemistry reactions. Its ability to participate in the formation of carbon-carbon bonds and other chemical transformations makes it a useful tool for the synthesis of complex organic molecules and the development of new chemical processes.
Used in Drug Discovery:
4-BROMO-7-METHYL-1H-INDOLE has been studied for its potential pharmacological activities, including its effects on the central nervous system. Researchers are exploring its potential use in treating various diseases, making it an important candidate in drug discovery efforts.
Used in Organic Synthesis Research:
4-Bromo-7-methyl-1H-indole is also used in the field of organic synthesis research, where its unique properties and reactivity are investigated to develop new synthetic methods and improve existing ones. This contributes to the advancement of organic chemistry and the discovery of novel compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 936092-87-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,0,9 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 936092-87:
(8*9)+(7*3)+(6*6)+(5*0)+(4*9)+(3*2)+(2*8)+(1*7)=194
194 % 10 = 4
So 936092-87-4 is a valid CAS Registry Number.

936092-87-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-BROMO-7-METHYL-1H-INDOLE

1.2 Other means of identification

Product number -
Other names 4-Bromo-7-methylindole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:936092-87-4 SDS

936092-87-4Relevant articles and documents

Povarov reaction, scope and limitations: Preparation of diversely heterocyclic tetrahydro-1H-cyclopenta[c]quinolines

Ni?o, Patricia,Caba, Marta,Aguilar, Nuria,Terricabras, Emma,Albericio, Fernando,Fernàndez, Joan-Carles

, p. 1117 - 1130 (2017/04/28)

Parallel synthesis of diverse heterocyclic-tetrahydro-1H-cyclopenta[c]quinolines in excellent yields and high endo diastereoselectivity has been described hereia These compounds are highly functionalized natural product-like tricyclic systems, which may be useful as biologically relevant targets. Fine tuning of the reaction conditions need to be performed depending on the nature and molecular structure of the heterocyclic aromatic carbaldehyde, as well as the choice of the Lewis acid catalyst. Synthesis of the heterocyclic aromatic aldehyde precursors of the Povarov Reaction is also described.

SUBSTITUTED TRICYCLIC COMPOUNDS WITH ACTIVITY TOWARDS EP1 RECEPTORS

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Page/Page column 120-121, (2013/10/22)

The present invention belongs to the field of EP1 receptor ligands. More specifically it refers to compounds of general formula (I) having great affinity and selectivity for the EP1 receptor. The invention also refers to the process for their preparation, to their use as medicament for the treatment and/or prophylaxis of diseases or disorders mediated by the EP1 receptor as well as to pharmaceutical compositions comprising them.

PYRIMIDINE DERIVATIVES AS PI3K INHIBITORS

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Page/Page column 93, (2008/06/13)

Thienopyrimidines of formula (Ia) or (Ib): wherein R1, R2, R3, are as defined in the claims.

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